State-selected reaction probabilities for the collinear reaction He+H~-(v)~HeH++H have been computed for v = 0-4 over a wide range of energies (to the dissociation limit), using the time-dependent wavepacket approach via time-energy mapping of the reactive flux. The results reproduce quantitatively
Semi-classical coupled wavepacket study of the dissociative charge exchange He+ + H2 → He+H+H+
✍ Scribed by François Aguillon
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 458 KB
- Volume
- 222
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
The semi-classical coupled wavepacket method is used to investigate the dissociative charge exchange reaction He+ +H2( IJ= O-4 ) +He + H + H+ and the vibronic excitation reaction He+ + H2( v= O-4) +He+ + Hz (u' ) . The center of mass collision energy ranges from 2 to 10 eV. The cross sections strongly depend on both the collision energy and the initial vibrational state. The results are interpreted in terms of wavepackets dynamics and compared to experimental results.
📜 SIMILAR VOLUMES
The previous quantum mechanical close-coupling study of the dissociative collisions in He + Hz (T-shape configuration) by the present authors [Chem. Phys. Letters 216 (1993) 6131 has been extended to a wide range of the total energy 4.8-7.5 eV. The dissociation process shows a clear vibrational enha
Classical trajectory calculations for the rotational excitation'of CO and Hz by collision &ith He have been carried out and compared to the accurate qu&~m mechanics1 cfculations of other workers The grecment is rasonably encourngig, although some irther&t limitations of this strictly classical appro